Hello. My husband is 1 year post ASCT and is doing well on Revlimid alone. (standard risk, lambda light chain disease). In the last month or so, he's been having very significant pain in his arms and neck. Of course musculoskeletal pain is listed among the many, many possible side effects of Revlimid, but I am wondering if others have experienced this. His blood markers look good and he has no other side effects from the Revlimid, so he'd like to continue on it if possible. He's doing the usual things one can do for pain. Thank you!

Hi, I hope everyone is doing well. I am writing this email inquiring about solutions for my mother, who is a MM patient. She has relapsed and is currently on a Dara KPD regimen. Her lesion has a soft tissue component that is pinching a nerve on the L5 vertebra and causing sciatica-type nerve pain in her right leg. She also feels numbness at the bottom of her right foot. The pain is very intense, and even painkillers are not helping. She is on weekly dex and that helps, but only for about a day. Please do help us with any information or suggestions that could help. She is unable to sit or walk and is in excruciating pain. Thank you for your time. Regards Rukmini Roy

Hi there, I would like to get in touch with a MM "Colleague" who is also diagnosed with t(4;14) which potentially qualifies as High Risk - and who has relapsed. What is your experience with treatment after relapse? Clinical Trials, regular treatment, etc. After nearly four years of MRD negative (as guessed by my physician; "guessed" because MRD is not allowed in Holland/Europe), I relapsed sometime in December 2022. At the moment, I am in a wait-and-see stage. My physician managed to make his/our hospital eligible for a clinical trial - MonumenTAL - a bispecific - from Janssen & Janssen. Although the M-Protien was low (3.7) at the last blood test, I feel that my body is slowly giving in to the pressure. I increasingly suffer from bone pain, especially in my hip. Anyway, hope somebody will share his or her experience. And maybe we can go through this ordeal together.

Wondering; to anyone on Medicare/Medicaid. Is it possible to have a Multiple Myeloma "Specialist", to work with the oncologist/haematologist? Will Medicare/Medicaid cover the cost? I have asked this a couple of times before this and I've yet to get an answer.

Hi all, wanted to provide an update and information on latest treatment option. Update and time for a new round of treatment. Over the past six months my Serum Kappa has been doubling and now has reached the threshold at over 100 to initiate a new course of action. My last visit at Moffit was looking at Talquetamab, ten-day hospital stay and follow up treatment. At Moffit yesterday under the expert care of the amazing Dr. Baz here is the new plan. Venetoclax, a selective BCL-2 inhibitor administered at home, Daratumumab, local oncologist administered with (Darzalex) showing really good results with my very specific translocation t(11;14). This specific translocation is present in only 15% of MM cases. Bone Marrow Biopsy to start in 10 days, PET scan a few other tests to follow. I’m feeling really positive with this plan. There always seems to be a new “plan B”. Keeping positive and hopeful, Peter

What are the main side effects you are experiencing? My partner with MM has a persistent cough and issues with his respiratory system. Thanks.

Has anyone tried Sea Moss? Friend is encouraging me to take this to help with inflamation, joint, digestive issues, and anti cancer effects. My friends mean well but I get neverous when it comes to herbs with smoldering myeloma.

My mom was recently diagnosed with multiple myeloma. She just finished her 2nd cycle of treatment. She is still experiencing a lot of back pain that wraps around to the front. Has anyone had this feeling and how long did it last before the treatments kicked in and lessened the pain? Her treatment is Daratumumab, Revlimid, and Dexamethasone.